Pharmaceutical compositions

ABSTRACT

The present invention relates to an improved mode of administration for cannabis and its natural and synthetic derivatives. A pharmaceutical composition suitable for sublingual aerosol or spray delivery of cannabis is provided. The formulation may be dispensed using a pump spray or the formulation may include a propellant, such as butane, 1,1,1,2-tetrafluoroethane (HFC-134a) or 1,1,1,2,3,3,3-heptafluoropropane (HFC-227). The term cannabis is used herein to refer to all physiologically active substances derived from the cannabis family of plants and synthetic cannabis analogues and derivatives, precursors, metabolites etc., or related substances having cannabis-like physiological effects.

RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.11/901,593, filed Sep. 18, 2007 now abandoned, which application is adivision of U.S. patent application Ser. No. 10/221,066, filed May 6,2003, now abandoned, which is a national stage filing under 35 U.S.C.§371 of international application PCT/GB01/01027, filed Mar. 9, 2001,which was published under PCT Article 21(2) in English, all of which areincorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to an improved mode of administration forcannabis and its natural and synthetic derivatives. The term cannabis isused herein to refer to all physiologically active substances derivedfrom the cannabis family of plants and synthetic cannabis analogues andderivatives, precursors, metabolites etc., or related substances havingcannabis-like physiological effects.

BACKGROUND OF THE INVENTION

The medicinal and psychoactive properties of the cannabis plant havebeen known for centuries. At present, cannabis is not legally available.However, there is growing pressure on politicians to legalise its use,especially for medicinal purposes.

Evidence suggests that cannabis is a safe, versatile and potentiallyinexpensive drug. It has been reported as being beneficial to patientssuffering from a wide range of symptoms experienced in connection withvarious, often very serious, medical conditions. For example, cannabishas been used to alleviate symptoms associated with cancer, anorexia,AIDS, chronic pain, spacicity, glaucoma, arthritis, migraine and manyother illnesses.

Cannabis is recognised as having anti-emetic properties and has beensuccessfully used to treat nausea and vomiting in cancer patientsundergoing chemotherapy.

Studies also report use of cannabis in treating the weight loss syndromeof AIDS and in reducing intraocular pressure for the treatment ofglaucoma. Cannabis is also reported to have muscle relaxing effects andanti-convulsant effects.

However, it is also well documented that these medicinal effects ofcannabis come at the cost of less desirable effects. It is alleged thatthe administration of cannabis causes changes in mood, perception andmotivation. The common euphoric effects have led to the use of cannabisas a recreational, “soft” drug and its criminalisation. The psychoactiveeffects are said to vary with dose, with the typical cannabis smokerexperiencing a “high” which lasts about 2 hours, during which there isimpairment of cognitive functions, perception, reaction time, learningand memory. These side effects clearly have implications, such as forthe operation of machinery, and in particular for driving. These effectsalso make cannabis less attractive for widespread, mainstream use, as itcan reduce a patient's ability to perform relatively simple tasks duringtreatment.

The euphoric effects of cannabis may also constitute an undesirable sideeffect for patients using the drug for medicinal purposes, especiallyfor “naive” cannabis users. Furthermore, here have been reports ofunpleasant reactions to cannabis, such as anxiety, panic orhallucinations. It is believed that these undesirable effects are mostcommonly associated with higher doses of cannabis.

Despite these effects, years of research have failed to show thatcannabis is dangerous. In fact, the results appear to have proved theopposite. Cannabis has been shown to be safer, with fewer serious sideeffects than most prescription drugs currently used as anti-emetics,muscle relaxants, hypnotics and analgesics, etc.

The physiological and pharmacological effects of cannabis depend upon anumber of factors, including the dosage level and the route ofadministration.

There are currently two main methods of cannabis delivery. Lung deliveryis most commonly achieved by smoking cannabis. Unfortunately, there areconcerns about the effect of this mode of administration on the lungs.Cannabis smoke carries even more tars and other particulate matter thantobacco, and so may be a cause of lung cancer. Furthermore, manypatients find the act of smoking unappealing, as well as generallyunhealthy. It is known that some of the chemicals produced by smokingcannabis are aggressive and smoking has been shown to cause the gradualdissolving of teeth. For these reasons, smoking is not an approvedmedical means of administration for any drug.

Attempts have been made to overcome some of the problems associated withsmoking both cannabis and tobacco by providing various smokelessinhalable aerosol formulations for lung delivery. A self-propelledinhalable aerosol of delta-9-tetrahydrocannabinol was developed as longago as 1975 as a bronchodilator. Inhalable aerosol formulations weremade comprising either only liquid components and or including a solidparticulate component carrying the active agent, such as the cannabis.The various formulations were found to be of varying effectiveness indelivering the active agent to the alveoli of the lungs in the samemanner as smoke.

However, both methods of lung delivery discussed above have been foundto cause a pronounced and involuntary cough, possibly from irritation ofthe trachea and lungs. This unpleasant side effect is not overcome bythe smoke-free method of lung delivery.

An oral dosage form of cannabis is available in the United States as aSchedule II drug. The capsules contain a synthetic version ofdelta-9-tetrahydrocannabinol (delta-9-THC), the main active substance incannabis, and they have had limited success for a number of reasons.Firstly, in light of its anti-emetic properties, the capsules arecommonly used to treat nausea and vomiting. Clearly, an oraladministration is not ideal as the patient may well have difficultykeeping the capsule down long enough for it to take effect. It has alsobeen found that orally administered THC is erratically and slowlyabsorbed into the bloodstream, making the dose and duration of actiondifficult to control. Furthermore, the oral dose is less effective thansmoked cannabis and therefore larger doses are required in order toachieve a desired therapeutic effect.

SUMMARY OF THE INVENTION

The applicants have discovered that an alternative mode ofadministration allows the clinical or medicinal effects of cannabis tobe maximised, whilst reducing the above discussed unpleasant andnegative side effects. According to the present invention, the cannabisis formulated for sublingual delivery in aerosol or spray form, whichoffers unexpected advantages over known modes of cannabis delivery. Theinvention also relates to a device for delivering such a composition asan aerosol or spray.

Formulations according to the invention may include a propellant or maybe dispensed using a pump spray device. The spray or aerosol devices mayhave upright or inverted valves. Furthermore, the aerosol or spraydevice may be adapted specifically for sublingual delivery. For example,the mouthpiece of the device may be adapted to direct the sprayed dosetowards the sublingual mucosa. The device may also be adapted todispense particles of a particular size, thereby optimising thesublingual uptake.

It is known that sublingual delivery of a pharmaceutically active agentresults in fast uptake. The active agent is administered to thesublingual mucosa, from which it is rapidly absorbed into thebloodstream. Sublingual delivery also avoids first-pass metabolism ofthe active agent.

Aerosol or spray delivery of a composition to the sublingual area isparticularly convenient and effective, and promotes fast-uptake. Thesprayed composition will be thinly spread over the sublingual area, sothat more of the dispensed composition will be absorbed and will beabsorbed more quickly than where sublingual delivery is by some othermode, such as, for example, allowing a tablet to dissolve under thetongue.

The fast onset of the therapeutic effects of sublingually administeredcannabis has the advantage of providing fast relief from the symptoms tobe treated. It also has the advantage of reducing the risk of excessivedoses being administered in an attempt to get immediate relief fromsymptoms, which is often observed in connection with slow-acting activeagents and means of administration and which is potentially dangerous.

Sublingual delivery is clearly more attractive than injection, asalternative method of delivery offering fast uptake. Injection ispainful, especially when regular administration is required. It can alsobe difficult for a patient to inject themselves, especially if weak orlacking co-ordination, often making it necessary for someone other thanthe patient to perform the administration.

Sublingual delivery also has advantages over oral delivery. It is wellsuited for administration of anti-emetics, it having rapid onset anddelivery is not affected by nausea and vomiting. A sublingual dose isalso absorbed at a predictable rate and so its administration can beaccurately controlled. Devices with metered valves may be used todispense the active agents sublingually, allowing accurate volumes, andtherefore accurate doses, to be dispensed.

Sublingual delivery also avoids the negative effects associated withsmoking. The risk of lung cancer due to the tar and impurities drawninto the lung by smoking will be avoided. Furthermore, the pronouncedand involuntary cough associated with lung delivery of cannabis is notexperienced with sublingual delivery.

A further and unexpected advantage associated with sublingual deliveryof cannabis is that it is significantly more effective than smoking(which in turn is known to be significantly more effective than oraldelivery). This is surprising in light of the huge surface area of thelungs which would be expected to allow much greater uptake of thecannabis than sublingual delivery which exposes a much smaller surfacearea to the active agent.

This effectiveness allows some of the undesirable effects of cannabisadministration to be avoided, these effects being mainly associated withlarger doses. Indeed, the applicants have discovered that the sublingualdelivery of cannabis allows the beneficial medicinal effects of cannabisto be enjoyed whilst minimising the negative effects, such as theeuphoria and impairment of faculties. That said, the sublingualadministration of doses of cannabis large enough to produce saideuphoric effect is still possible, if desired.

In one of the preferred embodiments of the present invention, apharmaceutical composition suitable for sublingual delivery is providedcomprising a pharmaceutically active agent which is cannabis and apropellant. The propellant may be, for example,1,1,1,2-tetrafluoroethane (HFC-134a), 1,1,1,2,3,3,3-heptafluoropropane(HFC-227) or butane. Most preferably, the propellant included in thecomposition is HFC-134a or HFC-227.

In the past, aerosol or spray formulations frequently included one ormore chlorofluorocarbon as a propellant, dichloro-difluoromethane beingcommonly used. It is well documented that chlorofluorocarbons areimplicated in the depletion of the ozone layer and their production,therefore, is being phased out. 1,1,1,2-tetrafluoroethane (HFC-134a) and1,1,1,2,3,3,3-heptafluoropropane (HFC227) are significantly less harmfulto the ozone layer and they are of low toxicity and of suitable vapourpressure for use as aerosol propellants, making then suitable for use inpharmaceutical aerosols. An additional benefit is that HFC-134a andHFC227 can be used in combination with many pharmaceutically activeagents, without causing any degradation to them or reducing theirphysiological activity. They are also not flammable.

Preferably, the composition of the present invention includes a carrier.In a preferred embodiment of the invention, the carrier is a lower alkyl(C₁-C₄) alcohol, a polyol, or a (poly) alkoxy derivative. Inembodiments, the carrier is a C₁-C₄ alkyl alcohol or a lanolin alcoholand, preferably, is ethanol or isopropyl alcohol. The most preferredalcohol is ethanol.

The preferred polyols include propylene glycol and glycerol and thepreferred (poly) alkoxy derivatives include polyalkoxy alcohols, inparticular 2-(2-ethoxyethoxy) ethanol (available under the TrademarkTranscutol®).

Further preferred (poly)alkoxy derivatives include polyoxyalkyl ethersand esters, such as polyoxyethylene ethers or esters. The preferredpolyoxyethylene ethers and esters are polyoxyethylene alkyl ethers,polyoxyethylene castor oil derivatives, polyoxyethylene sorbitan fattyacid esters and polyoxyethylene stearates.

The preferred fatty acid alkyl esters are ethyl oleate, isopropylmyristate and isopropyl palmitate. The preferred polyalkylene glycol ispolyethylene glycol.

In preferred embodiments, the inventive composition can comprise up to50% or, preferably, 25% w/w carrier. More preferred embodiments includebetween 3% and 15% w/w, or between 4 and 10% w/w carrier. Thepharmaceutical compositions can comprise between 50% and 99% w/w,preferably between 75% and 99% w/w, and, more preferably, between 88%and 95% w/w HFC-134a or HFC-227.

In further embodiments, compositions used in the present invention cancomprise a plurality of different carriers.

Further excipients can be included in the formulations employed in thepresent invention. For example, neutral oils as well as surfactants (thelatter for aiding the smooth operation of the valve), as are well knownto those skilled in the art, may be included.

Thus, in further preferred embodiments, compositions employed in theinvention can comprise an organic surfactant. The preferred organicsurfactant is oleyl alcohol, although others can be employed, includingsorbitan trioleate, sorbitan mono-oleate, sorbitan monolaurate,polyoxyethylene (20) sorbitan monolaurate, polyoxyethylene (20) sorbitanmono-oleate, natural lecithin, oleyl polyoxytheylene (2) ether, stearylpolyoxyethylene (2) ether, lauryl polyoxyethylene (4) ether, blockcopolymers of oxyethylene and oxypropylene, oleic acid, syntheticlecithin, diethylene glycol dioleate, tetrahydrofurfuryl oleate, ethyloleate, isopropyl myristate, glyceryl mono-oleate, glycerylmonostearate, glyceryl monoricinoleate, cetyl alcohol, stearyl alcohol,cetyl pyridinium chloride, olive oil, glyceryl monolaurate, corn oil,cotton seed oil or sunflower seed oil.

It is preferable to include a flavouring oil in a formulation to bedelivered sublingually. The preferred flavouring oil is peppermint oil,although it is clear that other flavour oils may be used, according topreference.

Some of the preferred compositions for the sublingual delivery accordingto the present invention contain tetrahydrocannabinols (THCs), such asdelta-9tetrahydrocannabinol, the major active constituent of cannabis.

Many of the readily available substances derived from the cannabis plantare extracted in liquid form which may itself be directly sprayed usinga pump spray or which may be soluble directly in the propellant, whilstother cannabis forms need to be solubilised in a co-solvent, such asethanol, thus causing or allowing all or a proportion of the activeagent present in the composition to dissolve and/or remain in solution,even after it has been dispensed.

The pharmaceutical compositions can be partial solutions in which only aproportion of the pharmaceutically active agent present therein isdissolved in the propellant and co-solvent, with the remainder being insuspension or suspendible. The exact proportions of dissolved andsuspended active agent will depend upon the active agent concerned, itsconcentration and the identity and quantity of the co-solvent (s) used.In preferred embodiments the compositions are in the form of liquidsolutions when maintained under pressure in devices in accordance withthe invention.

In a particularly preferred embodiment of the invention the compositioncomprises a solution of delta-9-tetrahydrocannabinol in ethanol as aco-solvent and HFC-134a as a propellant.

The compositions of the present invention may also comprise cannabis incombination with other pharmaceutically active agents. For example, aformulation particularly suitable for providing improved anti-emeticeffect comprises cannabis as the primary agent, with corticosteroid as asupplemental agent. In order to decrease toxicity of the primary agent,cannabis may be formulated together with the supplemental agentphenothiazine. Concurrent use of cannabis with prochlorperazine in lowdoses can reduce incidence of dysphoria which can accompany theadministration of cannabis.

According to a further aspect of the invention, devices for deliveringthe cannabis compositions of the first aspect of the invention areprovided.

Devices for administering metered aerosol doses of pharmaceuticalpreparations are well known in the art. Such devices include thosedisclosed in WO 92/11190, U.S. Pat. No. 4,819,834 and U.S. Pat. No.4,407,481. Many of these devices include metering valves havingcomponents formed from plastic materials, such as the valves availablefrom Bespak PLC of Bergen Way, Kings Lynn, Norfolk PE30 2JJ, UnitedKingdom, in which the valve core, metering chamber and some otherstructural components are formed from plastic materials. The plasticmaterials currently used for forming these structural parts in valvesemployed with many chlorofluorocarbon containing formulations includecertain acetal co-polymers.

Although the plastics employed to manufacture metering valves, includingthe aforementioned acetal co-polymers, have also been found to be stablein the presence of HFC-134a alone, the applicants, to their surprise,have determined that many of these plastics materials can be caused toswell in the presence of formulations which include certain carriers oractive agent solubilising co-solvents with HFC-134a. When such swellingtakes place in a valve, the fit of mutually slidable components, such asmetering chambers and valve cores, is adversely effected and they canbind together or become loose, causing the valve to leak or ceasefunctioning altogether.

This problem has now been solved by using a device for providingpharmaceutical doses comprising a container, filled with apharmaceutical composition including a pharmaceutically active agent ina solution of liquefied HFC-134a, or HFC-227, and a carrier selectedfrom pharmaceutically acceptable alcohols, polyols, (poly)alkoxyderivatives, fatty acid alkyl esters, polyalkylene glycols, anddimethylsulphoxide, and valve means arranged for delivering aerosoldoses of said pharmaceutical composition to the exterior of thecontainer, wherein at least a portion of the device is formed from apolyester. Preferably, the valve means includes at least one componentformed from a polyester, which component, more preferably, is a meteringchamber and/or a valve core.

In further embodiments, the container comprises a polyester and,preferably, consists of metal lined with a polyester. The canister capcan also be so formed.

Apart from allowing the aforementioned swelling problem to be solved, anadvantage of this aspect of the present invention is that use ofexpensive metal valve components can be avoided.

The preferred polyesters are polyalkylene benzene dicarboxylates, morepreferably polyalkylene terephthalates and, most preferably, apolybutylene terephthalate.

Such materials, preferably, have a density of about 1.3 g/cm³ and awater absorption of about 0.6% (23° C. saturation). The polyesters,also, are preferably partially crystalline in nature and have acrystalline melting range of 220-225° C.

Examples of suitable polybutylene terephthalates include those availableunder the Trademark Celanex® from Hoechst UK Limited, Walton Manner,Milton Keynes, Bucks MK7 7AJ, United Kingdom. Particularly preferred areCelanex® 2500 and Celanex® 500/2.

A variety of types of conventional spray devices exist are able todispense very accurate volumes. However, this alone cannot ensureadministration of a specific dose.

When pharmaceutical compositions are administered sublingually, it isparticularly important that they are accurately delivered to thesublingual area. The sublingual area is relatively small and can be hardto reach because of the position under the tongue. If the compositiondoes not come into contact with the sublingual mucosa, it will not bequickly absorbed and, indeed, may not be directly absorbed at all. Thiswill clearly lead to an inaccurate dose being administered and thepatient not receiving the desired amount of pharmaceutically activeagent.

Therefore, a problem associated with sublingual administration ofpharmaceutical compositions is the difficulty ensuring that apredictable dose is brought in contact with the sublingual mucosa. Thiscan be particularly problematic where the composition is delivered byspray delivery. There are various factors which particularly influencethe ability to ensure that a dispensed composition contacts therelatively small area of the sublingual mucosa.

Firstly, the direction and spread of the sprayed composition are clearlyrelevant. If the sprayed composition spreads or disperses upon leavingthe aerosol or spray device, it is likely to contact a large area of theoral cavity other than the sublingual mucosa. This will make it unlikelythat all of the composition will be absorbed and some of the activeagent will not have an effect, thereby effectively reducing the doseadministered.

Secondly, the velocity at which the composition is dispensed will alsoplay a role, as the sublingual mucosa will be relatively close to thedispensing device when in use. If the composition is travelling at highvelocity when it enters the oral cavity, it is more likely to spreadaround the cavity, rather than coming into contact almost exclusivelywith the sublingual mucosa, as desired.

At present there are no bespoke spray devices for sublingualadministration. Rather, conventional spray devices of various types aregenerally used, and the user must attempt to direct the spray to thesublingual area.

The majority of known, conventional spray devices basically comprise acontainer in which the composition is stored, the composition beingdispensed from an orifice or outlet, wherefrom it is allowed togenerally disperse, often creating a cloud of droplets of dispensedcomposition. When using such devices for sublingual delivery, the usercan, at best, attempt to control the general direction in which thecomposition is dispensed by pointing the device as a whole in a certaindirection. However, it will be difficult, if not impossible, to target asmall area like the sublingual mucosa, especially as it is positionedunder the tongue.

Many conventional spray devices use a propellant, wherein thecomposition is dispensed through a single orifice. This generallyresults in the composition being dispensed at high velocity which, asdiscussed above, is undesirable in sublingual spray delivery.

An example of a conventional spray device generally capable ofdispensing accurate doses is device is a so-called metered dose inhaler,or MDI device, frequently used to dispense pharmaceuticals for thetreatment of asthma or angina and which has an inverted valve. Aconventional MDI device comprises a pressurised aerosol container,carrying the composition to be administered for inhalation therapy. Thecontainer is encased in a housing which includes a mouthpiece and apassage leading from the orifice or outlet of the container to themouthpiece. The mouthpiece is shaped to be comfortably held between thelips when the pharmaceutical composition is dispensed.

The MDI devices currently available are specifically intended for lungdelivery. The dispensed composition is directed to the back of thethroat, and inhalation by the patient results in the composition beingdrawn into the lungs from the oral cavity. Whilst MDI devices candispense accurate and reproducible doses, such devices are not wellsuited to sublingual delivery for two reasons. Firstly, the devices areshaped to direct the dispensed substance to the back of the throat andnot under the tongue. Secondly, because the substance is inhaled, it isdispensed at high velocity.

Thus, in a preferred embodiment of the present application, a spray oraerosol device has a bespoke mouthpiece, the mouthpiece being adapted tochannel and direct the dispensed composition according to the presentinvention from an orifice of the device, towards the sublingual area ofthe user. Such a mouthpiece could be used in conjunction with aconventional spray device, such as one of the types discussed above.

Preferably, the mouthpiece of the dispensing device is angled inrelation to the main body of the device, so that the mouthpiece directsthe dispensed composition to the sublingual mucosa when the device isactivated whilst held in the normal position for use.

Such a mouthpiece could be used in conjunction with devices havingeither an upright or an inverted valve. In a preferred embodiment, thedevice has an inverted valve, such devices generally being capable ofdispensing accurate volumes of composition.

According to a further preferred embodiment, the mouthpiece fordirecting the dispensed composition to the sublingual area is part of ahousing in which the main body, including the container, of the spraydevice is held. The mouthpiece could be rigidly fixed with respect tothe housing, or the connection between the housing and the mouthpiececould be flexible, allowing the angle of the mouthpiece relative to themain body of the device to be adjusted.

In a further embodiment, the mouthpiece is shaped in such a way that itassists directional dispensing of the composition to the sublingual areaof the mouth.

Preferably, the mouthpiece is long enough to allow the opening of themouthpiece to sit under the tongue when the composition is dispensed.This will reduce the amount of composition being dispensed to parts ofthe oral cavity other than the sublingual area. Even more preferably,for greater comfort and greater ease of use, the mouthpiece is also aslim shape, fitting comfortably under the tongue or being comfortablyheld to direct the spray towards the sublingual area.

Additionally, the mouthpiece may also be shaped in such a way that itdiscourages the spread of the dispensed composition after it leaves themouthpiece. As discussed above, when a composition is dispensed by aconventional spray device it will generally spread, forming a cloud.This is undesirable where a small area of the oral cavity is to betargeted. In a preferred embodiment, the mouthpiece opening is no largerthan the average size of the sublingual area. This means that, despitesome degree of spreading of the dispensed composition after it has leftthe mouthpiece, the spread will be limited to ensure that the area ofthe oral cavity contacted by the dispensed composition will correspondgenerally to the sublingual area, provided the composition is dispensedin the correct direction.

It is also advantageous for the dispensing device to be adapted toreduce or control the velocity at which the dispensed composition leavesthe device. This will help to ensure that the composition comes intocontact with the sublingual mucosa and stays in contact for long enoughfor the pharmaceutically active agent to be absorbed. Such control maybe provided, to an extent, by the shape of the mouthpiece of thedispensing device.

Thus, in accordance with a further preferred embodiment of the presentinvention, the mouthpiece of the spray device has a cross-sectional areawhich first gradually increases, and then decreases. The resultant“duckbill” shape will both control the velocity of the dispensedcomposition and limit its spread. It is clear that a variety ofmouthpiece shapes may be used to reduce the velocity of the dispensedcomposition.

In another preferred embodiment, the velocity with which the compositionis dispensed is also reduced by providing the device with a plurality oforifices through which the composition is released. The provision ofmore than one orifice will reduce the force with which the dispensedcomposition is released from the main body of the device, therebyreducing its exit velocity. The more orifices through which thecomposition is dispensed, the slower the velocity of the substancedispensed.

In a yet more preferred embodiment, in a device having a plurality oforifices these orifices may be shaped and positioned to be directional,preferably serving to direct the individual jets of dispensedcomposition toward on another, to avoid unnecessary and undesirablespreading of the composition around the oral cavity.

Most preferably, the orifices are directed so that jets of dispensedcomposition converge at a point which is approximately the same distancefrom the nozzle of the device as the sublingual area will be from thenozzle when the device is used. Thus, the composition should contact arelatively small area, avoiding wastage caused by the composition beingdispensed to areas other than the sublingual mucosa.

In a preferred embodiment of the invention, the orifices of the deviceare further adapted to dispense particles of a particular size, therebyoptimising absorption across the sublingual mucosa.

A problem sometimes encountered with conventional spray and aerosoldevices is that there is some degree of interaction between thecontainer and the composition stored therein. This interaction can be inthe form of corrosion of the container by the composition, or leachingof materials from the container into the composition, both of which areclearly undesirable. Such interaction between the container and itscontents can significantly curtail the shelf life of the container.Furthermore, resultant contamination of the composition can bedangerous. Even seemingly inert compositions may eventually interactwith their container when stored for prolonged periods.

Such interaction between the container and the contents thereof is aparticular problem with the compositions of the present inventionbecause cannabis and its analogues and derivatives are highly corrosive.Thus, these compositions cannot be stored in convention metal containersfor any significant length of time.

It has been found that glass containers are considerably more resistantto interaction with compositions than the conventionally used metal andplastic containers. Therefore, in a further preferred embodiment of thepresent invention, the devices for spray dispensing the compositions ofthe invention include glass containers within which the composition isstored.

Preferably, in order to provide additional protection againstinteraction, the internal surface of the glass container may be coated.The coated containers will have surface properties like quartz, beinghighly inert. In a particularly preferred embodiment, the surface of theglass container is coated with a chemically bonded, ultra thin layer ofpure silicone oxide. The thickness of such a layer would preferably bebetween 0.1 and 0.2 microns. Such a layer may be applied by a processwhereby the inner surface of the container is first activated using pureoxygen. Next, silicone oxide coating gas is introduced into thecontainer. Then, a plasma reaction is initiated by microwave energy,leading to the formation of a silicon oxide layer on the inner surfaceof the glass container.

Clearly, other inert coatings applied to the glass container surface mayalso protect the glass from interaction with the composition to bestored therein. The effect of such coatings is particularly apparentover time, the coating providing an inert barrier between the glasscontainer and the composition stored therein.

A further advantage of glass containers is that it is much harder totamper with them than with conventional containers. The provision of atamper-proof container for pharmaceutical compositions as it will makeit very difficult to gain access to the composition. It is particularlydesirable to prevent extraction of the composition from the containerwhere the pharmaceutical composition is one which is open to abuse, likethe compositions of the present invention.

Containers made from conventional materials such as metals, such asaluminium, or plastics, are vulnerable to tampering. These materials maybe punctured, for example with a syringe, and the pharmaceuticalcomposition within the container can be extracted or material can beadded to the contents of the container. In some circumstances, suchtampering may even go unnoticed.

In contrast, glass cannot be punctured in this manner. Indeed, due toits tendency to break or shatter, it will be very difficult, if notimpossible to tamper with a glass container, without destroying thecontainer. A pressurised glass container in an aerosol or spray devicewill be particularly difficult to tamper with. Such containers will bepressurised, for example to a pressure of 6-8 bar and are prone toactually explode if tampered with, as the glass having a tendency tocrack or shatter, as discussed above. This will make it virtuallyimpossible for the contents of the container to be collected.

In order to reduce the risk of accidentally breaking of the relativelyfragile glass container during normal use, it is preferably encased in aprotective housing. Such a housing will reduce the risk of the containerbreaking by accident, for example when dropped.

One further advantage obviously afforded by using a container made fromglass is the fact that it is transparent. Thus, the contents of thecontainer are potentially visible. When the container is encased in ahousing, the housing could be provided with a window, or could betransparent itself, in order to allow the container contents to beviewed.

Being able to see the amount of the composition left in the containercan be very useful, especially where the composition is one which theuser relies upon heavily, so that it would be highly undesirable for thecomposition to unexpectedly run out. For example, where the containercontains a strong painkiller, it would be highly undesirable for thepatient to only realise that the composition has run out when theyrequire a further dose which is not available. Where the patient can seethe composition inside the container, it will be easier to ascertainwhen the supply of composition is about to run out and when it will benecessary to obtain more.

According to a preferred embodiment of the present invention, to furtherassist monitoring of the amount of composition left in a container, thecontainer is provided with markings to show how many doses are leftinside the container. Thus for example, a warning line is provided,indicating that it is time to obtain more composition when the levelinside the container reaches that line. Alternatively, where thecontainer is encased in a housing, the markings are on the housing,preferably adjacent to the container.

Some examples of devices for sublingual delivery of cannabis will now bedescribed, by way of example only, and with reference to the followingdrawings.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings are not intended to be drawn to scale. In thedrawings, each identical or nearly identical component that isillustrated in various figures is represented by a like numeral. Forpurposes of clarity, not every component may be labeled in everydrawing. In the drawings:

FIG. 1 is a cross sectional view of an embodiment of a device inaccordance with the invention, the device having an upright valve.

FIG. 2 is a cross sectional view of an embodiment of a housing,including a mouthpiece, for an inverted valve device, in accordance withthe present invention.

FIG. 3 is a view of the underside of the housing shown in FIG. 2.

FIG. 4 is a perspective view of the housing shown in FIG. 2.

FIG. 5 is a view down the mouthpiece of the housing shown in FIG. 2, thehousing containing a spray device with a nozzle having three orifices.

FIG. 6 is a side view of a device with an upright valve, and amouthpiece according to the present invention.

FIG. 7 is a perspective view of the device shown in FIG. 6, wherein thespray device is being activated by downward pressure on the top of thedevice.

DETAILED DESCRIPTION OF THE INVENTION

The device 1, shown in FIG. 1, comprises a substantially cylindricalcanister 2 sealed with a cap 3. Both the canister 2 and the cap 3 may bemanufactured from a variety of materials. Preferably, the canister andcap are formed from stainless steel or glass. This is because some ofthe cannabis substances which may be used in the present invention are“aggressive” chemicals and can attack “weaker” container materials. Thecanister and cap may be lined with a polyester (such as Celanex® 2500)or a lacquer (not shown).

A valve body moulding 4 comprises a cylindrical portion 5, which definesa metering chamber 6 and a stepped flange portion 7, and is formed byinjection moulding from Celanex® 2500. The stepped flange portion 7defines a first and outwardly facing annular seat 8 and a second,inwardly facing annular seat 9. The first annular seat 8 accommodates anannular sealing ring 10 and the second annular seat 9 accommodates afirst sealing washer 11. The first sealing washer 11 is located so as tocooperate with the cylindrical portion 5 of the valve body moulding 4,in defining the metering chamber 6.

A base 12 of the cylindrical portion 5 of the valve body moulding 4completes the boundary to the metering chamber 6 and provides a seat fora second sealing washer 13.

The sealing ring 10 and the first and second sealing washers 11 and 13can be formed from a butyl rubber, neoprene or one of the elastomersdisclosed for such purposes in WO 92/11190.

An elongate, substantially cylindrical and partially hollow valve core14 is slidably located within the first and second sealing washers 11and 13 and extends through an orifice 15, defined in the base 12. Thevalve core 14 is formed by injection moulding from Celanex® 2500.

A stepped inlet passage 16 communicates between a first end 17 of thevalve core 14 and an inlet orifice 18, formed through the side of thevalve core 14. In a likewise manner, an outlet passage 19 communicatesbetween the second end 20 of the valve core 14 and an outlet orifice 21formed through the side of the valve core 14. An annular flange 22extends radially outwardly from the valve core 14 between the inlet andoutlet orifices 18 and 21 and adjacent to the outlet orifice 21.

A stainless steel compression coil spring 23 acts between the annularflange 22 and the second sealing washer 13, urging the annular flange 22into contact with the first sealing washer 11, such that the outletorifice 21 lies inside the first sealing washer 11 and is therebyisolated from the metering chamber 6. In this position, as shown in FIG.1, the inlet orifice 18 is located within the metering chamber 6. Aflexible tube 24 is engaged within the stepped inlet passage 16 andextends from the valve core 14 to the base of the canister 2 (as shownin FIG. 1). Thus, the inlet orifice 18 is in communication with a regionwithin the canister 2 adjacent to its base 12.

The cap 3 is firmly attached to the canister 2 by crimping and, thus,holds the assembly of the valve body moulding 4, valve core 14, coilspring 23, sealing washers 11 and 13 and sealing ring 10 in place asshown in FIG. 1, with the sealing ring 10 and first sealing washer 11sufficiently compressed to seal the interior of the device 1 and preventthe egress of its contents.

Downward movement of the valve core, in the direction of arrow A,against the action of the spring 22 will bring the outlet orifice 21into the metering chamber immediately after the first orifice 18 hasbeen sealed from the metering chamber 6 by the second sealing washer 13.

When filled with a composition in accordance with the present invention,as shown at 25, the device 1 will provide metered doses of thecomposition when used as follows. The device 1 should be held in theposition shown in FIG. 1, so that the composition 25, by virtue of itspressure, enters the metering chamber 6 via the tube 24, the inletpassage 16 and the inlet orifice 18. Subsequent depression of the valvecore 14, in the direction of arrow A, seals the inlet orifice 18 andhence the remainder of the canister 2, from the metering chamber 6 andopens the outlet passage to the metering chamber 6, via the outletorifice 21. Since the composition 25 in the metering chamber 6 ispressurised with the propellant, it will be expelled from the meteringchamber 6 through the outlet orifice 21 and the outlet passage 19. Ifthe valve core 14 is then allowed to return to the position shown inFIG. 1, under the influence of the spring 22, the outlet orifice 21 isagain sealed from the metering chamber 6 and the metering chamber 6 willbe filled with pressurised composition 25 from the canister 2, via thetube 24, stepped inlet passage 16 and inlet orifice 18.

Whilst the foregoing description relates to a device having an uprightvalve, it is clear that devices with inverted valves may also be used todispense the compositions of the present invention. Typical suppliers ofinverted valves include Bespak plc, King's Lynn, UK, 3M Neotechnic,Clitheroe, UK and Valois Pharm, Le Vaudreuil, France.

FIGS. 2 to 7 show a mouthpiece according to a preferred embodiment ofthe present invention. In FIGS. 2 to 5, the mouthpiece 100 isillustrated as being part of the housing 102 which is used to house aninverted valve spray device. In FIGS. 6 and 7, the mouthpiece 200 isused with a conventional upright valve device 202 and is affixed to themoveable button part 204 of the dispensing device.

Thus, when the device is in use, the moveable button 204 is depressedand the mouthpiece will also move relative to the main body of thedispensing device.

Upon activating either type of spray device illustrated in the figures,the composition held within the container is dispensed from the spraydevice. As it leaves the spray device, the dispensed composition entersthe mouthpiece. The mouthpiece then channels the composition to theopening of the mouthpiece 106.

In use, the mouthpiece is preferably placed under the tongue, with theopening of the mouthpiece adjacent to the sublingual area. This ensuresthat the dispensed composition contacts, almost exclusively, thesublingual area when it leaves the mouthpiece.

The figures illustrate the preferred shape of the mouthpiece. Themouthpiece has a smooth shape, with a gradually increasingcross-sectional area which then decreases again towards the opening.

In FIG. 5, the orifices 300 of the dispensing device are shown. Thereare three orifices, and each is directional, so that the jets ofcomposition dispensed therefrom converge at a predetermined distancefrom the outlets themselves.

There now follow some examples of compositions according to the presentinvention.

Example 1

A composition comprising delta-9-tetrahydrocannabinol (delta-9-THC) withHFC134a suitable for use in a device as described above can beformulated from the following ingredients:

Component percent w/w g/can Delta-9-THC 0.7 0.099 Ethanol 96% BP 13.21.866 Peppermint oil 1.4 0.205 HFC-134a 84.7 12.02 Total 100 14.19

The peppermint oil is added to the delta-9-THC/ethanol solution andmixed thoroughly. 2.17 g of the resulting solution is then placed in thecanister 2 and the valve assembly, comprising the valve body moulding 4,first sealing washer 11, second sealing washer 13, spring 22, tube 23,and annular seal 10 are then sealed onto the canister 2 as shown in FIG.1 by the cap 3. The propellant is then added to the canister by beingforced through the valve core 14 at great pressure, and the completedevice is then checked for leaks.

Example 2

A second composition comprising delta-9-THC with HFC-134a suitable foruse in a device as described above can be formulated from the followingingredients:

Component percent w/w g/can Delta-9-THC 0.164 0.010 Ethanol 96% BP 4.9920.305 HFC-134a 94.844 5.795 Total 100 6.11

The delta-9-THC is dissolved in the ethanol in the proportions set outabove and 0.315 g of the resulting solution is then placed in a canister2 and a valve assembly, comprising a valve body moulding 4, firstsealing washer 11, second sealing washer 13, spring 22, tube 23, andannular seal 10, is then sealed onto the canister 2 by crimping as shownin FIG. 1 by the cap 3. The propellant (HFC-134a) is then added to thecanister, by being forced through the valve core 14 at great pressure,and the complete device is then checked for leaks. After the propellantentered the canister it dissolves the remaining portions of thecomposition.

Example 3

A third composition comprising delta-9-THC and suitable for use in adevice as described above can be formulated from the followingingredients:

Component percent w/w g/can Delta-9-THC 0.164 0.010 Ethanol 96% BP 7.50.458 HFC-134a 92.336 5.641 Total 100 6.11

The delta-9-THC is dissolved in the ethanol in the proportions set outabove and 0.315 g of the resulting solution is then placed in a canister2. A valve assembly (as described in Example 2) is then sealed onto thecanister 2 by crimping and the HFC-134a propellant is then added to thecanister, by being forced through the valve core 14 at great pressure,and the complete device is then checked for leaks. After the propellantentered the canister it dissolves the remaining portions of thecomposition.

Example 4

Further compositions comprising delta-9-THC with HFC-134a, suitable foruse in a device as described herein, can be formulated in accordancewith the details set out in the following table, in which all figuresare given on a percent by weight basis.

Formulation A B C D E delta-9-THC 0.164 0.164 0.164 0.164 0.164Transcutol 9.984 4.992 Oleyl alcohol 2.496 Propylene glycol 4.992Ethanol 4.992 7.488 4.992 20.51 p134a 89.852 89.852 89.852 89.852 79.326Total 100 100 100 100 100

Formulations A-E are prepared using a similar technique to that set outin Example 2 above. Briefly, the delta-9-THC is dissolved with the otherexcipient or excipients (excepting the HFC-134a) and the resultingsolution is then placed in a canister 2. A valve assembly is then sealedonto the canister 2 by crimping and the HFC-134a propellant is thenadded to the canister 2, by being forced through the valve core 14 atgreat pressure. After the propellant enters the canister 2, it dissolvesthe remaining portions of each composition.

Although only delta-9-tetrahydrocannabinol is referred to in the abovementioned examples, other cannabis active agents previously discussed inthis application may be substituted therefor in quantities which woulddissolve at least partially in the propellant/co-solvent mixture.

What is claimed is:
 1. A metered valve pump spray device consistingessentially of a liquid cannabis extract, in carriers consistingessentially of propylene glycol, and ethanol, wherein said metered valvepump spray device is adapted to spray a dose towards a patient'ssublingual mucosa from the orifice of the device, and is adapted todispense particles of a particular size, thereby optimizing thesublingual uptake in the patient.